tecfor care GmbH
DE-MF-000007722 · Germany · Gummersbach
tecfor care GmbH is registered in the European database on medical devices as a manufacturer, with 143 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 143 |
|---|
Most frequent device types declared: Electric medical bed, Stand-up aids, Zubehör Seitengitter, bed extension.
Among these devices, 37 are declared active.
Devices declared under this manufacturer
- Aufrichter zweigeteilt für Standardbetten RAL 9006
- Aufrichter zweigeteilt für Standardbetten RAL 9023
- Bettverlängerung für Ecofit Xtra 140
- Dreigeteiltes Seitengitter Alu mit Kunststoffabdeckung in grau
- Dreigeteiltes Seitengitter Stahl 815/mm
- Durchgehendes Seitengitter Holz 1970mm Referenzdekor Lindberg Eiche
- Durchgehendes Seitengitter Holz 1973mm Referenzdekor Kirsche Havanna
- Durchgehendes Seitengitter Holz 1973mm Referenzdekor Weissbuche
- Durchgehendes Seitengitter Holz 1983mm Referenzdekor Weissbuche
- Durchgehendes Seitengitter Holz 1983mm Referenzdekor Whiteriver Eiche
- Ecofit Plus mit Seitengitter Buche
- Ecofit S 100
Showing 12 of 143 declared devices.
Catalogue references include 00010, 00110, 01318, 01681, 04815, 04818.
European nomenclature codes declared: V08068001, V08060101, V08068099.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 143 |
| Country of registration | Germany |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 143 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.
North American profile: Neither register. tecfor care GmbH was not found in either the U.S. or the Canadian register.